Today,
January 10, was my father's birthday. He would've been 88 years old. February
14 is the third anniversary of his death. The passing of Janet's father on
December 1 reopened the wound. My brother is taking my mom to the mausoleum to
visit my dad. I asked him tell my dad that I loved him and missed him even
though I feel silly asking him to speak to a brass plaque on a wall on my
behalf. He says it's not silly although I honestly disagree but am having him
do it at my request anyway.
If you're not interested in the thoughts of an opinionated, liberal, differently abled, alternative lifestyle woman, then don't read on.
Sunday, January 13, 2013
HBD DAD
Saturday, December 22, 2012
Not a happy time
I
normally am involved in the holiday season getting a tree, shopping for gifts
and helping Janet decorate. This year, I
just can't get into the spirit. Too many
things have happened in my life and all around me: the death of Janet’s dad,
her mom's illness, the elementary school shooting, Hurricane Sandy and the Fiscal
Cliff. I'm not only not festive, I'm
depressed.
The
elementary school shooting in Connecticut is horrific…The loss of 20 young lives
and their generations' loss of innocence. When I was growing up, I felt safe in
my elementary school even when I thought the outside world was going
crazy. It was stable and secure inside
James H. Johnson Elementary School -- who could imagine a crazed person killing
my classmates?
Wednesday, December 12, 2012
Memories of Josh
Janet's father, Josh Tye Williams Jr., passed over a little
after midnight on December 1, 2012. Before he passed, his family had a
wonderful opportunity to spend time with him when he was mentally with it. They
were able to have some positive interaction with him. The memorial gathering and
the military funeral were very low-key and simple and would've been to his
liking. After all the events of the day, some of us went out to lunch and spent
more time remembering him.
I feel a need to share some special memories of Josh,
perhaps selfishly, so that I can change the picture of him that is stuck in my head…
Of him snapping at me, although I have so many more positive thoughts about
him.
I have many memories of Josh; Of him being annoyed with his
computer and trying to help him with it, of him sitting in his big black
recliner watching TV really loud, of him cooking, of him sneaking me little
pieces of country ham before it was served and of having casual conversation
with him and his dry, occasionally biting sense of humor. The most important
ones to me though were of him at our handfasting. He was one of three males in
attendance and the other two were under the age of seven. My father was not
feeling very positive about my life choices at the time so none of my family was
in attendance. I started to explain this to the gathering when Josh loudly
announced that this was not a problem because I was now a member of the
Williams family. I immediately went over and kissed him right on top of the
head! I think I knocked off his hat. During the party afterwards, I remember Josh
dancing from one group of women to the next. I can see him now, a straw wide
brimmed hat on, moving from group to group, not really dancing with anyone,
just having a good time.
I think we have a picture of him dancing in our handfasting
photo album and I wanted to add it to the photo boards that Janet and Terry,
her mom, were making for the memorial but I didn't think of it until after they
were done. But I think I achieved my goal, I now have a snapshot in my head of
him dancing with his hat on amongst the lesbians…
Tuesday, October 2, 2012
47% uneditted
When my MS
symptoms started to get progressively worse over my 10 years of working at the
college, I saw importance in publicly struggling with my disability. Although I
tried to hide the most personal aspects of my illness, I felt that I was
perhaps one of the few working disabled people that students and staff might be
exposed to and I wanted to be a strong example. A coworker sometimes referred
to me as The Face of MS. I was proud of this role that I played. In retrospect,
I realize that I may be making myself out to be some sort of heroic martyr in
this blog post, but it's how I genuinely felt.
Mr. Romney cannot be President of the United States and only recognize half of the population of the country. I hope that the 47% and their friends and family will vote on November 6 and show him that his attitude and statements are unacceptable and not befitting the leader and chief of the country.
Sunday, September 23, 2012
disenfranchised unedited
My mother was a stay-at-home mom and I spent a lot of time
with her when I was little. When election time rolled around she always took me
with her when she voted. I remember her picking me up in the voting booth so I
could make her selections. This is a strangely poignant memory for me. Her
civic mindedness rubbed off on me.
I was very alarmed when threats to the voting process moved close
to home, to the neighboring state of Pennsylvania. Pennsylvania is joining the
growing list of states that are attempting to disenfranchise their populace.
Pennsylvania is requiring that all voters provide a different form of picture
ID beyond what they've ever had to show. This change will primarily affect the
elderly, disabled and poor who don't have the money or means to get the new
identification. The methods of identification that have been used for years
will no longer be sufficient. Those that will primarily be affected are
traditionally Democratic demographic groups.
I agree that the current security conscious climate requires
additional steps to be taken to protect the voting process. However, this
change should not take place a few months before a major presidential election,
causing large numbers of people to potentially be unable to vote.
This situation is not unique to Pennsylvania. Texas
attempted to pass a similar voter ID law, but it was overturned in appeals
court on the grounds that it was unfair to the lower income and minority
voters.
Wednesday, September 12, 2012
Mrs. Romney's MS unedited
I was
watching the news a few days ago and they were discussing how Romney is
defending himself against the accusations that he is out of touch with the
experiences of average Americans. Mrs. Romney said that they were very aware of
struggle like the average person because they deal with her MS. I know MS is
difficult to deal with for anyone, but her statement really got my goat.
I really
don't believe that the experiences of a chronically ill multimillionaire are
even vaguely similar to the experience of the average person with this illness.
Mrs. Romney has practically unlimited resources at her disposal whereas the
average person must depend on insurance to meet their health needs. As I've
said often before, insurance companies view a patient with chronic illness as
someone who will not benefit from many services and treatments because they
will show no improvement. Thus these services and treatments are not medically
necessary.
For example,
Mrs. Romney can afford a home health aide out-of-pocket if there is a problem
with the insurance. An average American with insurance receives home health
aide service for a limited period of time from the date of the onset of the
disease. Someone on Medicare receives this service for an unlimited period of
time, but only three times a week. In another example, although physical
therapy is known to be beneficial to an MS patient according to doctors and
physical therapists, insurance companies find it to be not medically necessary.
If the patient cannot afford to pay a physical therapist out-of-pocket or make
other arrangements, they will not receive this necessary treatment. These are
just two of many examples I could give that show that a patient with unlimited
resources has an advantage over someone reliant on insurance, Medicare or
Medicaid.
From its
initial onset, the progression of MS is different in each patient. The level of
disability, the symptoms and the speed at which it progresses varies from
person to person. I have the most severe form, chronic progressive multiple
sclerosis and I've been dealing with the various symptoms for over 20 years.
Clearly from observing Mrs. Romney in her various public speaking events, she
has a very mild form.
I don't
doubt that Mrs. Romney faces many challenges because of her disease and I don't
want to give the impression that I wish her ill. But as a multimillionaire, her
experiences cannot compare to those who have the illness but have limited
resources. I think Mr. and Mrs. Romney be to find some other way to prove some
point of commonality with the average citizen. Their struggles are not mine.
Wednesday, August 22, 2012
PACs uneditted
Because I am bedbound and have a lot of blocks of free time,
of course I end up watching a lot of television. The political advertisements
have been driving me crazy, but more so than in previous election times and for
different reasons. Janet has mentioned her dislike of the advertisements on
both sides because of the backstabbing and muckraking. Of coarse, I don't find
these qualities redeeming but I've noticed something else about the
advertisements that bothers me even more.
After about 7 PM every night, each grouping of advertising
includes at least one pro-Romney or anti-Obama commercial. The majority are not
directly sponsored by Romney’s campaign, but are paid for by different
Republican Political Action Committees (PACs). These PACs are run by various
influential Republican multimillionaires and billionaires. Because of political
campaign funding laws, these multimillionaires and billionaires are limited as
to how much they can fund Romney's campaign directly, but they can "
hide" behind these groups and support their candidate on a much larger
scale.
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